(Q84505783)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20589934%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH (English)

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6 February 2020

8

Peter Lichter

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6 February 2020

3

Gudrun Göhring

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6 February 2020

author name string

Inka Praulich

1

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6 February 2020

Marcel Tauscher

2

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6 February 2020

Stefanie Glaser

4

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6 February 2020

Winfried Hofmann

5

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6 February 2020

Simone Feurstein

6

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6 February 2020

Christian Flotho

7

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6 February 2020

Charlotte M Niemeyer

9

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6 February 2020

Brigitte Schlegelberger

10

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6 February 2020

Doris Steinemann

11

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6 February 2020

publication date

1 October 2010

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Genes, Chromosomes and Cancer

6 February 2020

published in

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6 February 2020

volume

49

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6 February 2020

issue

10

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6 February 2020

page(s)

885-900

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Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells

6 February 2020

cites work

1 reference

7 January 2021

Genomic microarrays in human genetic disease and cancer

1 reference

7 January 2021

Leukemic cluster growth in culture is an independent risk factor for acute myeloid leukemia and short survival in patients with myelodysplastic syndrome

1 reference

7 January 2021

Apoptosis is a Common Histopathological Finding in Myelodysplasia: the Correlate of Ineffective Haematopoiesis.

1 reference

7 January 2021

Epigenetic inactivation of a RAS association domain family protein from the lung tumour suppressor locus 3p21.3.

1 reference

7 January 2021

Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH.

1 reference

7 January 2021

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

1 reference

7 January 2021

High-resolution array comparative genomic hybridization of single micrometastatic tumor cells.

1 reference

7 January 2021

Reduced c-Myb activity compromises HSCs and leads to a myeloproliferation with a novel stem cell basis

1 reference

7 January 2021

Identification of small gains and losses in single cells after whole genome amplification on tiling oligo arrays

1 reference

7 January 2021

Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.

1 reference

7 January 2021

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

1 reference

7 January 2021

PRV-1 mRNA expression discriminates two types of essential thrombocythemia

1 reference

7 January 2021

Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype

1 reference

7 January 2021

Myelodysplastic and myeloproliferative disorders in children.

1 reference

7 January 2021

A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases.

1 reference

7 January 2021

Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics

1 reference

7 January 2021

Molecular mechanisms of myelodysplastic syndrome

1 reference

7 January 2021

Analysis of array-CGH data using the R and Bioconductor software suite

1 reference

7 January 2021

Apoptosis and antiapoptotic mechanisms in the progression of myelodysplastic syndrome

1 reference

7 January 2021

Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH.

1 reference

7 January 2021

Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia

1 reference

7 January 2021

Acquired mutations in TET2 are common in myelodysplastic syndromes

1 reference

7 January 2021

Single-cell chromosomal imbalances detection by array CGH

1 reference

7 January 2021

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

1 reference

7 January 2021

Whole genome scanning as a cytogenetic tool in hematologic malignancies

1 reference

7 January 2021

FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q)

1 reference

7 January 2021

Cytogenetic profile of myelodysplastic syndromes with complex karyotypes: an analysis using spectral karyotyping

1 reference

7 January 2021

Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes

1 reference

7 January 2021

Novel TET2 mutations associated with UPD4q24 in myelodysplastic syndrome.

1 reference

7 January 2021

Chromosomal deletions in the myelodysplastic syndrome

1 reference

7 January 2021

Genomic analysis of acute leukemia

1 reference

7 January 2021

Myelodysplastic syndrome in children and adolescents.

1 reference

7 January 2021

[Myelodysplastic diseases in childhood]

1 reference

7 January 2021

High-resolution genomic arrays facilitate detection of novel cryptic chromosomal lesions in myelodysplastic syndromes

1 reference

7 January 2021

Clinical and morphological features of paediatric myelodysplastic syndromes: a review of 34 cases

1 reference

7 January 2021

Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR

1 reference

7 January 2021

A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation?

1 reference

7 January 2021

Acute myeloid leukemia with a complex aberrant karyotype is a distinct biological entity characterized by genomic imbalances and a specific gene expression profile

1 reference

7 January 2021

High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage

1 reference

7 January 2021

Optimization and evaluation of single-cell whole-genome multiple displacement amplification.

1 reference

7 January 2021

High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival.

1 reference

7 January 2021

Assessment of differentiation and progression of hepatic tumors using array-based comparative genomic hybridization

1 reference

7 January 2021

Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease

1 reference

7 January 2021

High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemia

1 reference

7 January 2021

Automated screening for genomic imbalances using matrix-based comparative genomic hybridization.

1 reference

7 January 2021

AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes

1 reference

7 January 2021

Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20797

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20589934%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

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